Spread of herpes simplex virus type 1 in the central nervous system during experimentally reactivated encephalitis

Because many of the features of reactivated herpes simplex virus type 1 (HSV-1) central nervous sytems (CNS) infections in vivo are incompletely understood, we used an animal model to study the development of the morphological, ultrastructural, radiological and immunological changes which occurred d...

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Veröffentlicht in:Microbial pathogenesis 1990-02, Vol.8 (2), p.119-134
Hauptverfasser: Stroop, William G., McKendall, Robert R., Battles, Emma-Jean M.M., Schaefer, Douglas C., Jones, Barbara
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container_end_page 134
container_issue 2
container_start_page 119
container_title Microbial pathogenesis
container_volume 8
creator Stroop, William G.
McKendall, Robert R.
Battles, Emma-Jean M.M.
Schaefer, Douglas C.
Jones, Barbara
description Because many of the features of reactivated herpes simplex virus type 1 (HSV-1) central nervous sytems (CNS) infections in vivo are incompletely understood, we used an animal model to study the development of the morphological, ultrastructural, radiological and immunological changes which occurred during acute and experimentally reactivated diseases. Rabbits were intranasally inoculated with HSV-1, and their latent trigeminal ganglionic and CNS infections were reactivated by intravenous injection of cyclophosphamide and dexamethasone. Technetium brain scans were performed to localize areas of blood-brain barrier breakdown, and cerebrospinal fluid (CSF) was analysed for IgG content by radial immunodiffusion assays. Nervous system tissues were studied by in situ hybridization and by immunofluorescent, light and electron microscopic techniques. Diffuse uptake of technetium was observed as HSV-1 spread transsynaptically into the brain during the acute phase of infection, and viral antigens and nucleic acids were detected in both the CNS olfactory and trigeminal systems. During latency, viral RNA was detected in the nuclei of neurons within the CNS olfactory cerebral and entorhinal cortices, indicating that HSV-1 became latent within the same CNS structures that were involved during the acute phase of infection. Following drug-induced reactivation, the brain scans revealed a more focal breakdown of the blood-brain barrier, and both neurons and neuronal processes in the entorhinal and olfactory cortices contained viral nucleic acids which correlated with the ultrastructural presence of HSV-1 virions. During the reactivated phase of infection a marked increase in the CSF IgG index occurred without an increase in the CSF: serum albumen ratio indicating a prompt intrathecal response in infected rabbits as compared to controls. To some extent, the CSF IgG index reflected the degree of histopathological damage.
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Psychology</topic><topic>Herpes Simplex - cerebrospinal fluid</topic><topic>Herpes Simplex - microbiology</topic><topic>herpes simplex virus</topic><topic>HSV-1</topic><topic>IgG</topic><topic>immunoglobulins</topic><topic>Microbiology</topic><topic>Nucleic Acid Hybridization</topic><topic>Rabbits</topic><topic>Radionuclide Imaging</topic><topic>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</topic><topic>RID</topic><topic>RNA</topic><topic>Simplexvirus - pathogenicity</topic><topic>Virology</topic><topic>Virus Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stroop, William G.</creatorcontrib><creatorcontrib>McKendall, Robert R.</creatorcontrib><creatorcontrib>Battles, Emma-Jean M.M.</creatorcontrib><creatorcontrib>Schaefer, Douglas C.</creatorcontrib><creatorcontrib>Jones, Barbara</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stroop, William G.</au><au>McKendall, Robert R.</au><au>Battles, Emma-Jean M.M.</au><au>Schaefer, Douglas C.</au><au>Jones, Barbara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spread of herpes simplex virus type 1 in the central nervous system during experimentally reactivated encephalitis</atitle><jtitle>Microbial pathogenesis</jtitle><addtitle>Microb Pathog</addtitle><date>1990-02-01</date><risdate>1990</risdate><volume>8</volume><issue>2</issue><spage>119</spage><epage>134</epage><pages>119-134</pages><issn>0882-4010</issn><eissn>1096-1208</eissn><coden>MIPAEV</coden><abstract>Because many of the features of reactivated herpes simplex virus type 1 (HSV-1) central nervous sytems (CNS) infections in vivo are incompletely understood, we used an animal model to study the development of the morphological, ultrastructural, radiological and immunological changes which occurred during acute and experimentally reactivated diseases. Rabbits were intranasally inoculated with HSV-1, and their latent trigeminal ganglionic and CNS infections were reactivated by intravenous injection of cyclophosphamide and dexamethasone. Technetium brain scans were performed to localize areas of blood-brain barrier breakdown, and cerebrospinal fluid (CSF) was analysed for IgG content by radial immunodiffusion assays. Nervous system tissues were studied by in situ hybridization and by immunofluorescent, light and electron microscopic techniques. Diffuse uptake of technetium was observed as HSV-1 spread transsynaptically into the brain during the acute phase of infection, and viral antigens and nucleic acids were detected in both the CNS olfactory and trigeminal systems. During latency, viral RNA was detected in the nuclei of neurons within the CNS olfactory cerebral and entorhinal cortices, indicating that HSV-1 became latent within the same CNS structures that were involved during the acute phase of infection. Following drug-induced reactivation, the brain scans revealed a more focal breakdown of the blood-brain barrier, and both neurons and neuronal processes in the entorhinal and olfactory cortices contained viral nucleic acids which correlated with the ultrastructural presence of HSV-1 virions. During the reactivated phase of infection a marked increase in the CSF IgG index occurred without an increase in the CSF: serum albumen ratio indicating a prompt intrathecal response in infected rabbits as compared to controls. To some extent, the CSF IgG index reflected the degree of histopathological damage.</abstract><cop>Oxford</cop><pub>Elsevier India Pvt Ltd</pub><pmid>2161485</pmid><doi>10.1016/0882-4010(90)90076-3</doi><tpages>16</tpages></addata></record>
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subjects Animals
Antibodies, Viral - cerebrospinal fluid
Biological and medical sciences
Brain - diagnostic imaging
Brain - microbiology
Brain - pathology
brain scan
cerebrospinal fluid
CSF
DNA
Encephalitis - cerebrospinal fluid
Encephalitis - microbiology
Female
Fundamental and applied biological sciences. Psychology
Herpes Simplex - cerebrospinal fluid
Herpes Simplex - microbiology
herpes simplex virus
HSV-1
IgG
immunoglobulins
Microbiology
Nucleic Acid Hybridization
Rabbits
Radionuclide Imaging
Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains
RID
RNA
Simplexvirus - pathogenicity
Virology
Virus Activation
title Spread of herpes simplex virus type 1 in the central nervous system during experimentally reactivated encephalitis
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